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ViewForum R6.3V1 - SFDA Registration ME0000003237SFDAA00053

Access comprehensive regulatory information for ViewForum R6.3V1 in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000003237SFDAA00053 and manufactured by Philips Medical Systems Nederland B.V..

This page provides complete registration details including product category (Medical Device), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.

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SFDA Official Data
Class IIa
ME0000003237SFDAA00053
ViewForum R6.3V1
SFDA Registration: ME0000003237SFDAA00053
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Product Information

Image Processing Software

Product Use

ViewForum software receives image data from medical scanning devices, such as CT and MRI, or from image archives. ViewForum performs viewing, image manipulation, communication, printing, and quantification of images.

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000003237SFDAA00053
Authorization ID
GHTF-2017-1142
Status
Active
Expire Date
February 01, 2023
Manufacturer
Model Information
Model ID(s)
Version 6.3.X.XX
Product Accessories

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